4H,6H-Indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazinium, 5a,10b-dihydro-2-[2,4,6-tris(1-methylethyl)phenyl]-, (5aS,10bR)-, tetrafluoroborate(1-) (1:1)

97%

Reagent Code: #37075
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CAS Number 1827720-97-7

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Weight 503.3830 g/mol
Formula C₂₇H₃₄BF₄N₃O
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description Product Description

This compound is primarily utilized in organic synthesis as a chiral catalyst, particularly in asymmetric reactions where high enantioselectivity is required. Its structure, featuring a rigid indeno-triazolo-oxazinium core, enables effective control over stereochemistry in the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the production of a single enantiomer is critical for activity or efficacy. Additionally, its tetrafluoroborate counterion enhances solubility and stability in various organic solvents, making it suitable for use in a wide range of reaction conditions.

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inventory 50mg
10-20 days ฿5,742.00

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4H,6H-Indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazinium, 5a,10b-dihydro-2-[2,4,6-tris(1-methylethyl)phenyl]-, (5aS,10bR)-, tetrafluoroborate(1-) (1:1)
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This compound is primarily utilized in organic synthesis as a chiral catalyst, particularly in asymmetric reactions where high enantioselectivity is required. Its structure, featuring a rigid indeno-triazolo-oxazinium core, enables effective control over stereochemistry in the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the production of a single enantiomer is critical for activity or efficacy. Additionally, its tetraf

This compound is primarily utilized in organic synthesis as a chiral catalyst, particularly in asymmetric reactions where high enantioselectivity is required. Its structure, featuring a rigid indeno-triazolo-oxazinium core, enables effective control over stereochemistry in the formation of complex molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the production of a single enantiomer is critical for activity or efficacy. Additionally, its tetrafluoroborate counterion enhances solubility and stability in various organic solvents, making it suitable for use in a wide range of reaction conditions.

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